Last synced on 14 November 2025 at 11:06 pm

ViaOne Epicardial Access System

Page Type
Cleared 510(K)
510(k) Number
K243928
510(k) Type
Traditional
Applicant
CardioVia Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
90 days
Submission Type
Summary

ViaOne Epicardial Access System

Page Type
Cleared 510(K)
510(k) Number
K243928
510(k) Type
Traditional
Applicant
CardioVia Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
90 days
Submission Type
Summary